Komlósi K - Search Results

1

Phenotypic manifestations of the OCTN2 V295X mutation: sudden infant death and carnitine-responsive cardiomyopathy in Roma families.

Melegh B, Bene J, Mogyorósy G, Havasi V, Komlósi K, Pajor L, Oláh E, Kispál G, Sumegi B, Méhes K. Melegh B, et al. Among authors: komlosi k. Am J Med Genet A. 2004 Dec 1;131(2):121-6. doi: 10.1002/ajmg.a.30207. Am J Med Genet A. 2004. PMID: 15487009

2

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency.

Komlósi K, Magyari L, Talián GC, Nemes E, Káposzta R, Mogyorósy G, Méhes K, Melegh B. Komlósi K, et al. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S15-9. doi: 10.1007/s10545-009-0926-1. Epub 2009 Feb 24. J Inherit Metab Dis. 2009. PMID: 19238580

3

No influence of SLC22A4 C6607T and RUNX1 G24658C genotypic variants on the circulating carnitine ester profile in patients with rheumatoid arthritis.

Komlósi K, Talián GC, Faragó B, Magyari L, Cserép V, Kovács B, Bene J, Havasi V, Kiss CG, Czirják L, Melegh B. Komlósi K, et al. Clin Exp Rheumatol. 2008 Jan-Feb;26(1):61-6. Clin Exp Rheumatol. 2008. PMID: 18328148

4

Plasma carnitine ester profiles in Crohn's disease and ulcerative colitis patients with different IGR2230a_1 genotypes.

Talián G, Lakner L, Bene J, Komlósi K, Horváth K, Gasztonyi B, Miheller P, Figler M, Mózsik G, Tulassay Z, Melegh B. Talián G, et al. Among authors: komlosi k. Int J Immunogenet. 2009 Dec;36(6):329-35. doi: 10.1111/j.1744-313X.2009.00834.x. Epub 2009 Sep 7. Int J Immunogenet. 2009. PMID: 19735486

5

[Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family].

Komlósi K, Bene J, Havasi V, Tihanyi M, Herczegfalvi A, Móser J, Melegh B. Komlósi K, et al. Orv Hetil. 2004 Aug 29;145(35):1805-9. Orv Hetil. 2004. PMID: 15493224 Hungarian.

6

Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation.

Komlósi K, Kellermayer R, Maász A, Havasi V, Hollódy K, Vincze O, Merkli H, Pál E, Melegh B. Komlósi K, et al. Pathol Oncol Res. 2005;11(2):82-6. doi: 10.1007/BF02893371. Epub 2005 Jul 1. Pathol Oncol Res. 2005. PMID: 15999151 Free article.

7

Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn's disease.

Bene J, Magyari L, Talián G, Komlósi K, Gasztonyi B, Tari B, Várkonyi A, Mózsik G, Melegh B. Bene J, et al. Among authors: komlosi k. World J Gastroenterol. 2006 Sep 14;12(34):5550-3. doi: 10.3748/wjg.v12.i34.5550. World J Gastroenterol. 2006. PMID: 17006998 Free PMC article.

8

Histopathologic abnormalities of the lymphoreticular tissues in organic cation transporter 2 deficiency: evidence for impaired B cell maturation.

Komlósi K, Havasi V, Bene J, Süle N, Pajor L, Nicolai R, Benatti P, Calvani M, Melegh B. Komlósi K, et al. J Pediatr. 2007 Jan;150(1):109-111.e2. doi: 10.1016/j.jpeds.2006.09.042. J Pediatr. 2007. PMID: 17188629

9

Prevalence of SLC22A4 1672T and SLC22A5 -207C combination defined TC haplotype in Hungarian ulcerative colitis patients.

Magyari L, Bene J, Komlósi K, Talián G, Faragó B, Csöngei V, Járomi L, Sáfrány E, Sipeky C, Lakner L, Varga M, Gasztonyi B, Melegh B. Magyari L, et al. Among authors: komlosi k. Pathol Oncol Res. 2007;13(1):53-6. doi: 10.1007/BF02893441. Epub 2007 Mar 27. Pathol Oncol Res. 2007. PMID: 17387389 Free article.

10

Plasma carnitine ester profiles in Crohn's disease patients characterized for SLC22A4 C1672T and SLC22A5 G-207C genotypes.

Bene J, Komlósi K, Magyari L, Talián G, Horváth K, Gasztonyi B, Miheller P, Figler M, Mózsik G, Tulassay Z, Melegh B. Bene J, et al. Among authors: komlosi k. Br J Nutr. 2007 Aug;98(2):345-50. doi: 10.1017/S0007114507705020. Epub 2007 Mar 29. Br J Nutr. 2007. PMID: 17391561

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